Canonical Allele Identifier: CA1677459290

Gene: PRKN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161350116G= , CM000668.2:g.161350116G=	GRCh38
NC_000006.11:g.161771148G= , CM000668.1:g.161771148G=	GRCh37
NC_000006.10:g.161691138G=	NCBI36
NG_008289.1:g.1382687C=
NG_008289.2:g.1382687C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000338468.8:c.1259C=	ENSP00000343589.4:n.1259C=
ENST00000366894.6:c.1140C=	ENSP00000355860.2:n.1140C=
ENST00000366898.6:c.1381C= MANE Select	ENSP00000355865.1:p.His461=
ENST00000673871.1:c.1462C=
ENST00000674006.1:n.766C=
ENST00000674436.1:n.1017C=
ENST00000338468.7:c.808C=	ENSP00000343589.3:p.His270=
ENST00000366894.5:c.808C=	ENSP00000355860.1:p.His270=
ENST00000366896.5:c.934C=	ENSP00000355862.1:p.His312=
ENST00000366897.5:c.1297C=	ENSP00000355863.1:p.His433=
ENST00000366898.5:c.1381C=	ENSP00000355865.1:p.His461=
ENST00000479615.5:c.*157C=	ENSP00000434414.1:n.*157C=
ENST00000610470.4:c.514C=	ENSP00000483773.1:p.His172=
NM_004562.2:c.1381C=	NP_004553.2:p.His461=
NM_013987.2:c.1297C=	NP_054642.2:p.His433=
NM_013988.2:c.934C=	NP_054643.2:p.His312=
XM_011535863.1:c.1378C=	XP_011534165.1:p.His460=
XM_017010908.1:c.1495C=	XP_016866397.1:p.His499=
XM_017010909.2:c.1141C=	XP_016866398.1:p.His381=
XM_024446449.1:c.1144C=	XP_024302217.1:p.His382=
XR_001743443.2:n.1573C=
NM_004562.3:c.1381C= MANE Select	NP_004553.2:p.His461=
NM_013987.3:c.1297C=	NP_054642.2:p.His433=
NM_013988.3:c.934C=	NP_054643.2:p.His312=